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Health-Related Quality of Life in Children with Hypoplastic Left Heart Syndrome: Changes over Time and Associations
Karen Uzark1, Sunkyung Yu2, Katherine Afton2
1University of Michigan Mott Children's Hospital, Ann Arbor, MI.
Insights
Health-related quality of life (HRQOL) in children with hypoplastic left heart syndrome declines over time, independent of cardiac issues. Neurodevelopmental problems are linked to poorer HRQOL, necessitating routine assessments.
Area of Science:
- Pediatric Cardiology
- Developmental Pediatrics
- Quality of Life Research
Background:
- Hypoplastic left heart syndrome (HLHS) is a severe congenital heart defect requiring complex management.
- Long-term outcomes for HLHS survivors include challenges beyond cardiac health, impacting overall well-being.
- Understanding health-related quality of life (HRQOL) trends and influencing factors is crucial for comprehensive care.
Purpose of the Study:
- To assess changes in parent-reported HRQOL over time in children with HLHS.
- To investigate the relationship between neurodevelopmental and clinical factors and patient-reported HRQOL in HLHS survivors.
Main Methods:
- A longitudinal cohort study involving 165 HLHS survivors from the Single Ventricle Reconstruction (SVR) trial follow-up.
- The Pediatric Quality of Life Inventory (PedsQL) was administered to parents at two time points (SVR II and SVR III).
- Univariate analyses examined associations between clinical/neurodevelopmental measures and concurrent PedsQL scores.
Main Results:
- Parent-reported PedsQL scores significantly decreased across all domains between median ages of 6.1 and 10.9 years.
- The proportion of children with "at risk" impaired HRQOL increased in all domains.
- No significant correlations were found between medical variables and HRQOL, but neurodevelopmental dysfunction correlated with worse HRQOL.
Conclusions:
- HRQOL in HLHS children declines with age, irrespective of cardiac status.
- Neurodevelopmental dysfunction is a significant correlate of diminished patient-reported HRQOL.
- Routine neurodevelopmental and HRQOL assessments are vital for targeted interventions.
Objectives:
To evaluate changes in health-related quality of life (HRQOL) over time as perceived by parents and to examine associations between neurodevelopmental and clinical factors and patient-reported HRQOL in a large multicenter cohort of children with hypoplastic left heart syndrome.
Study Design:
Longitudinal/cohort. The Pediatric Quality of Life Inventory (PedsQL) was administered to 163 parents/165 Fontan survivors enrolled in the Single Ventricle Reconstruction (SVR) trial follow-up studies. In addition to examination of changes in parent-reported HRQOL over time, univariate associations between clinical and neurodevelopmental measures and concurrent self-reported PedsQL scores were evaluated.
Results:
Despite no significant change in reported heart problems/cardiac symptoms, PedsQL scores reported by parents decreased between SVR II (median age: 6.1 years, interquartile range: 6.0-6.2) and SVR III (median age: 10.9 years, interquartile range: 10.4-11.4) across all domains: total P < .001, physical P = .02, psychosocial P < .001, emotional P < .001, social P ≤ .001, and school P < .001. There was a corresponding increase in proportions with "at risk" impaired HRQOL: total 28% to 39%, physical 27% to 39%, psychosocial 25% to 40%, emotional 20% to 34%, social 22% to 31%, and school 21% to 38%. While there were no significant correlations between medical variables and self-reported PedsQL scores, neurodevelopmental dysfunction across multiple measures was significantly correlated with worse self-reported HRQOL.
Conclusions:
By parent report, HRQOL in children with hypoplastic left heart syndrome decreases over time unrelated to their cardiac symptoms and complications. Neurodevelopmental dysfunction is associated with worse patient-reported HRQOL. Routine assessment of neurodevelopmental function and HRQOL is essential to inform interventions to improve outcomes.
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